WO2016077282A1

WO2016077282A1 - Antiviral effects of narasin in swine feed

Info

Publication number: WO2016077282A1
Application number: PCT/US2015/059848
Authority: WO
Inventors: Thomas Alan MARSTELLER; Jane Granville Owens; Christopher Leigh PULS; Matthew John RITTER; Kelly Shern ROSENKRANS; Thomas Edmund WEBER
Original assignee: Eli Lilly And Company
Priority date: 2014-11-13
Filing date: 2015-11-10
Publication date: 2016-05-19
Also published as: JP2017536345A; ES2754354T3; US20170296504A1; CL2017001207A1; MX2017006264A; CN107106534B; TWI656872B; CA2963476A1; AU2015346616B2; EA031870B1; EP3217971A1; BR112017006307A2; PL3217971T3; CN107106534A; EP3217971B1; KR20170066622A; EA201790831A1; CA2963476C; PT3217971T; AU2015346616A1

Abstract

The present invention relates to a composition for ameliorating viral infections in nursery pigs. The composition contains the polyether ionophore narasin, and is supplied to the nursery pigs in an orally-acceptable form. The composition is effective in reducing viral shedding and the severity of diarrhea after challenge of nursery pigs with Porcine Epidemic Diarrhea Virus (PEDV).

Description

ANTIVIRAL EFFECTS OF NARASIN IN SWINE FEED

The present invention relates to compositions containing narasin and methods of using narasin to treat a nursery pig for porcine epidemic diarrhea virus infection.

The present invention is in the field of treatment of symptoms associated with porcine epidemic diarrhea virus (PEDV) infection. PEDV is a coronavirus which causes mortality in up to 100% of infected piglets, but has limited mortality in older swine. More than 10,000 piglets may die each day in the United States from PEDV. Thus, PEDV is having a significant economic impact on the price and availability of pork products.

Two PEDV vaccines are currently being marketed in the United States. Both vaccines have been approved for use in pregnant sows which may provide passive immunity to nursing piglets through antibodies in the sows' milk. However, the efficacy of these vaccines has yet to be demonstrated, the vaccines must be administered to sows individually through injection, and the levels of maternally-derived antibodies begin to decline after closure of a piglet's gut to macromolecule absorption.

Narasin is a polyether ionophore produced by Streptomyces spp, and can be purified from cultures of S. lydicus and S. granuloruber. Narasin has been approved by regulatory authorities in many countries to increase weight gain in growing- finishing swine. Narasin has been shown to block replication of the flavivirus responsible for dengue fever when added to cultured human cells infected with the virus (Low, et al., Antiviral Therapy 16: 1203-18, 2011). However, when administered with feed, narasin has been reported to be toxic to nursery pigs when supplied at a concentration of about 83 mg/kg feed, at least in the presence of tiamulin.

New treatments for PEDV are needed, especially a therapy which would provide protection to a pigs after weaning, such as a nursery pig.. A therapy which can be administered orally to a number of animals at once would also be advantageous. Because PEDV has been shown to be transmitted by aerosolized virus, a therapy which would decrease shedding of virus from infected swine would facilitate containment of the disease caused by this virus.

Accordingly, the present invention provides a method of treating a nursery pig for PEDV infection, comprising administering to said pig narasin with an orally-acceptable carrier. The orally-acceptable carrier is selected from the group comprising an animal feed, a liquid composition other than an animal feed, and a solid composition other than an animal feed. The concentration of narasin used in this method is selected from the group of about 30 mg/kg, about 40 mg/kg, about 50 mg/kg, or about 60 mg/kg of the orally-acceptable carrier. The present invention also provides a method of treating a nursery pig for PEDV infection, comprising administering to said pig narasin with an orally-acceptable carrier, wherein the orally-acceptable carrier is selected from the group comprising an animal feed, a liquid composition other than an animal feed, and a solid composition other than an animal feed, and wherein the concentration of narasin is selected from the group of about 30 mg/kg, about 40 mg/kg, about 50 mg/kg, and about 60 mg/kg of the orally-acceptable carrier.

The present invention also provides a method of treating a nursery pig for PEDV infection, comprising administering to said pig narasin with an animal feed, wherein the concentration of narasin may be about 30 mg/kg, about 40 mg/kg, about 50 mg/kg, or about 60 mg/kg of the orally-acceptable carrier. The present invention also provides a method of treating a nursery pig for PEDV infection, comprising administering to said pig narasin with an animal feed, wherein the concentration of narasin is about 60 mg/kg of the orally-acceptable carrier.

Further, the present invention provides narasin for use in the treatment of PEDV infection in a nursery pig. Narasin may be supplied to the nursery pig as a composition with an orally-acceptable carrier such as, for example without limitation, an animal feed, a liquid composition other than an animal feed, or a solid composition other than an animal feed. The concentration of narasin present in this composition may be about 30 mg/kg, about 40 mg/kg, about 50 mg/kg, or about 60 mg/kg of the orally-acceptable carrier. The present invention also provides narasin for use in the treatment of PEDV infection in a nursery pig, wherein narasin is administered with an animal feed and the concentration of narasin is about 30 mg/kg to about 60 mg/kg of the animal feed. The present invention also provides narasin for use in the treatment of PEDV infection in a nursery pig, wherein narasin is administered with an animal feed and the concentration of narasin is about 60 mg/kg of the animal feed.

Further, the present invention provides narasin with an orally-acceptable carrier for use in the treatment of PEDV infection in a nursery pig, wherein the orally-acceptable carrier comprises an animal feed, a liquid composition other than an animal feed, or a solid composition other than an animal feed, and wherein the concentration of narasin may be about 30 mg/kg, about 40 mg/kg, about 50 mg/kg, or about 60 mg/kg of the orally-acceptable carrier. Further, the present invention also provides narasin with an animal feed for use in the treatment of PEDV infection in a nursery pig, wherein the concentration of narasin is about 30 mg/kg to about 60 mg/kg of the animal feed. Further, the present invention also provides narasin with an animal feed for use in the treatment of PEDV infection in a nursery pig, wherein the concentration of narasin is about 60 mg/kg of the animal feed.

Further, the present invention provides the use of narasin in the preparation of a medicament for the treatment of PEDV infection in a nursery pig. The medicament may be a composition comprising narasin with an orally-acceptable carrier such as, for example without limitation, an animal feed, a liquid composition other than an animal feed, or a solid composition other than an animal feed. The concentration of narasin present in this composition may be about 30 mg/kg, about 40 mg/kg, about 50 mg/kg, or about 60 mg/kg of the orally-acceptable carrier. Further, the present invention provides the use of narasin in the preparation of a medicament for the treatment of PEDV infection in a nursery pig, wherein the medicament is narasin with an animal feed and the concentration of narasin is about 30 mg/kg to about 60 mg/kg of the animal feed. Further, the present invention provides the use of narasin in the preparation of a medicament for the treatment of PEDV infection in a nursery pig, wherein the medicament is narasin with an animal feed and the concentration of narasin is about 60 mg/kg of the animal feed.

Further, the present invention provides for a composition which provides an antiviral effect to a nursery pig, wherein the composition comprises a concentration of narasin and an orally-acceptable carrier. The orally-acceptable carrier may comprise an animal feed, a liquid composition other than an animal feed, or a solid composition other than an animal feed. The concentration of narasin in the above composition may be about 30 mg/kg, about 40 mg/kg, about 50 mg/kg, or about 60 mg/kg of the composition.

Further, the invention provides for a composition which provides an antiviral effect to a nursery pig, wherein the composition comprises a concentration of narasin with an animal feed, wherein the concentration of narasin is about 30 mg/kg to about 60 mg/kg of the animal feed. Further, the invention provides for a composition which provides an antiviral effect to a nursery pig, wherein the composition comprises a concentration of narasin with an animal feed, wherein the concentration of narasin is about 60 mg/kg of the animal feed.

Further, the present invention provides for a composition comprising a concentration of narasin and an orally-acceptable carrier, said composition providing an antiviral effect to a nursery pig, wherein the orally-acceptable carrier is selected from the group of an animal feed, a liquid composition other than an animal feed, and a solid composition other than an animal feed, and wherein the concentration of narasin may be about 30 mg/kg, about 40 mg/kg, about 50 mg/kg, and about 60 mg/kg of the orally- acceptable carrier.

Narasin and methods of making and using narasin as a useful therapeutic against gram-positive bacteria, anaerobic bacteria, and fungi, as an anticocccidial agent, and as an agent for increasing feed utilization in ruminants, are recited in U.S. Pat No. 4,038,384 (published July 26, 1977), U.S. Pat. No. 4,309,504 (published Jan. 5, 1982), and U.S. Pat. No. 4,342,829 (published Aug. 3, 1982). See also Berg et al., J. Antibiot. 31 : 1-6 (1978) and "Narasin, a new polyether antibiotic: discovery and fermentation studies, Chapter 38, pages 471-485, volume 18, Developments in Industrial Microbiology [a publication of the Society for Microbiology (1977)].

As used herein, the terms "treating", "to treat", or "treatment", include restraining, slowing, stopping, reducing, ameliorating, or reversing the progression or severity of an existing symptom, disorder, condition, or disease. A treatment may be applied prophylactically or therapeutically.

As used herein, "nursery pig" is a pig which has been weaned but is not yet a growing-finishing pig. Weaning of pigs typically occurs at about three weeks of age (about 21 days old) but can occur as early as one week (about seven days old) and as late as six weeks of age (about 42 days old). A weaned pig no longer solely relies on a sow's milk for sustenance but rather consumes solid feed compositions.

As used herein, "growing- finishing swine" are pigs of at least about 50 pounds of body weight, or about ten weeks of age. The terms "growing-finishing," grow- finish," and "grower- finisher" are synonymous. The term "swine" includes any member of the genus Sus. As used herein, "animal feed" includes edible materials which are consumed by livestock for the materials' nutritional value. Animal feed includes feed rations, e.g. compositions that meet an animal's nutritional requirements, and also include

compositions that do not meet an animal's nutritional requirement.

In an embodiment, the composition comprises an orally-acceptable carrier for narasin. An "orally-acceptable carrier" includes any physiologically acceptable carrier suitable for oral administration. Orally-acceptable carriers include, without limitation, animal feed compositions, aqueous compositions, and liquid and solid compositions suitable for use in animal feed products and/or for oral administration to an animal.

Suitable carriers are known in the art, and include those described in U.S. Patent

6,780,628.

The following experimental example is illustrative of the use of narasin to reduce viral shedding or ameliorate symptoms of viral infection in nursery pigs. The invention is not limited to this specific illustrative example or to any preferred embodiment, and the invention could apply to treatments for other viruses, such as porcine reproductive and respiratory syndrome (PRRS) virus, porcine circovirus (PCV), or a porcine coronavirus.

Example 1

Experimental Design

Eighty-one weaning stage (21.8 +/- 0.6 days) commercial crossbred piglets (Wilson's Prairie View Farms, Burlington, WI) free of PEDV infection arrived at the site and six were used as potential replacement animals during the pre-challenge period (Day -7 to Day 0). Six piglets were removed at Day 0 immediately prior to PEDV challenge, resulting in fifteen pens containing five piglets/pen (n = 75) animals. There were five pens per treatment. For balance of sentinel piglets within a block, a total of thirty-nine piglets of one gender and thirty-six of the other gender were used. The use of five pens (twenty- five piglets) per treatment group was estimated to detect significant differences (P < 0.10) between treatment groups in growth performance and incidence of viral shedding.

The seventy-five piglets were randomly assigned to one of three treatment groups: control (no ionophore), narasin (30mg/kg) and narasin (60mg/kg). They acclimatized to their environment and were fed daily for seven days prior to exposure with PEDV on Day 0. Treatment continued for 14 days following challenge. Pigs from the three treatment groups were administered orally with 4xl0⁴ TCID₅o/mL of the PEDV isolate

PEDV/USA/NC/2013/49469 (College of Veterinary Medicine, Iowa State University). The piglets were monitored daily for changes in clinical parameters, , clinical score for diarrhea, depression and gauntness, rate of food consumption, and rate of body weight change and viral swabs were taken daily to determine viral shedding.

Statistical Methods

Viral shedding values was evaluated by RMANOVA and the PROC MIXED procedure of SAS (SAS, Cary, NC). Other variables for analysis included growth performance data (average daily gain, or ADG; average daily feed intake, or ADFI; and feed efficiency (unit of weight gain per unit of feed consumed), or G:F), incidence and severity of diarrhea, depression, and gauntness scores, and intestinal histology score and immunohistochemistry. The analysis of the growth performance outcomes were conducted using a generalized linear mixed model and the PROC MIXED procedure of SAS.

Incidence and severity of the score data (diarrhea, depression, and gauntness) were summarized by frequencies and mean scores on a daily basis.

Diet Formulations

Diet formulations were manufactured at Provimi (Lewisburg, OH) and fed in meal form. Composition of diets were analyzed by Minnesota Valley Testing Laboratories (New Ulm, MN), and nutrient analysis values were found to be similar to formulated levels. Narasin levels were analyzed by Covance Laboratories (Greenfield, IN) and were found to be 0, 29.8, and 64.1 mg/kg, which were similar to formulated levels of 0, 30, and 60 mg/kg, respectively.

No ractopamine (last feed drug) was detected in the experimental diets.

Growth Performance

The effects of narasin inclusion level on mean body weights (BW), average daily weight gain (ADG), average daily feed intake (ADFI), feed efficiency (G:F), and feed conversion ratio (F:G) are shown in Table 1. Table 1. Least-squares means for the effects of narasin inclusion level growth performance of nursery pigs challenged with PEDV

Narasin inclusion level, mg/kg

Item 0 30 60 SEM -value

No. of pens 5 5 5 - -

BW, lb

Day -7¹ 14.3 14.9* 14.9* 0.72 0.04

Day O² 16.6 16.9 16.7 0.68 0.72

Day 5³ 18.1 18.7 19.2 0.78 0.12

Day 14⁴ 26.5 26.9 26.9 1.01 0.92

ADG, lb

Day -7 to 0 0.32 0.29 0.26* 0.017 0.08

Day 0 to 5 0.24 0.38* 0.48* 0.056 0.03

Day 5 to 14 0.94 0.92 0.85 0.066 0.61

Day 0 to 14 0.65 0.70 0.70 0.047 0.74

ADFI, lb

Day -7 to 0 0.36 0.37 0.36 0.032 0.67

Day 0 to 5 0.65 0.68 0.71 0.035 0.51

Day 5 to 14 1.23 1.23 1.22 0.102 1.00

Day 0 to 14 0.99 1.00 1.01 0.069 0.98

G:F, lb:lb

Day -7 to 0 0.882 0.802 0.742 0.0755 0.40

Day 0 to 5 0.375 0.551 0.670* 0.0767 0.05

Day 5 to 14 0.772 0.772 0.708 0.0609 0.59

Day 0 to 14 0.659 0.711 0.698 0.0486 0.73

F:G, lb:lb

Day -7 to 0 1.14 1.33 1.38 0.112 0.22

Day 0 to 5 3.80 1.93 1.56 0.744 0.12

Day 5 to 14 1.30 1.38 1.42 0.114 0.64

Day 0 to 14 1.52 1.48 1.44 0.106 0.85

Means are significantly different than control treatment (P < 0.10).

!Day -7: Animal arrival to test facility; allotment to study. Includes extra 6 pigs. 2Day 0: Pigs challenged with PEDV.

Day 5: Sentinel animal (1 pig/pen) removed from pen, euthanized, and necropsied. 4Day 14: End of study.

Feeding 30 and 60 mg/kg narasin numerically increased overall ADG (7.7% and

7.7%, respectively) and G:F (7.9% and 5.9%, respectively) compared to the control (0 mg/kg).

Feeding 30 and 60 mg/kg narasin increased (P < 0.10) ADG (58.3% and 100%, respectively) in the Day 0 to 5 period (Table 1) compared to the control, although feeding 60 mg/kg narasin resulted in a decreased (P < 0.10) ADG (18.8%) in the Day -7 to 0 period. In addition, feeding 60, but not 30 mg/kg narasin, increased (P < 0.10) G:F in the Day 0 to 5 period (78.7%) compared to 0 mg/kg narasin. There were no statistical differences for ADG, ADFI, G:F, or F:G in the Day 5 to 14 period. There was no effect (P > 0.10) of narasin level on overall (Day 0 to 14) growth performance.

Clinical Scoring

Table 2 indicates the scoring system used to measure diarrhea, depression, and gauntness. Table 3 compares the mean scores for diarrhea, depression and gauntness in nursery pigs whose diet included 0, 30 or 60 mg/kg narasin.

Table 2. Enteric Clinical Observation Scoring System

Clinical

Evaluation Clinical Signs

1 = Normal (no diarrhea present)

2 = Pasty (semi-solid; cow-pie consistency)

Diarrhea

3 = Semi-liquid (loose with some solid material ; oatmeal consistency)

4 = Liquid (watery feces with little or no solid material)

0 = Normal (bright, alert, and responsive)

1 = Mild (may stand isolated but will quickly respond to stimulation)

Depression 2 = Moderate (may stand isolated with head down and possible signs of muscle weakness; delayed response to stimulation)

3 = Severe (severely depressed; recumbent and reluctant to rise)

0 = Normal abdominal fill; flank is full and round

Gauntness 1 = Decreased gut fill; flank is flat

2 = Severely gaunt; flank is hollow

The mean of diarrhea scores measured over the 14-d period decreased numerically with increasing narasin level (1.49, 1.45, and 1.37 for 0, 30, and 60 mg/kg, respectively). Severity of diarrhea decreased with increasing narasin level (3.16, 2.72, and 2.48 for 0, 30, and 60 mg/kg, respectively; Table 3).

The mean of depression scores measured over the 14-d period was not affected by narasin level, however, a low incidence of depression observed in animals is noted (5, 4, and 3 animals for 0, 30, and 60 mg/kg narasin, respectively). Severity of depression decreased with increasing narasin level, although this was based on relatively few animals exhibiting the condition (Table 3). There was little effect of narasin level on mean or severity of gauntness scores measured over the 14-d period (Table 3).

Table 3. Means for the effects of narasin inclusion level on diarrhea scores of nursery pigs challenged with PEDV

Narasin inclusion level, mg/kg

Item 0 30 60

No. of pens 5 5 5

Diarrhea score

Mean of Day O to 14 1.49 1.45 1.37

Severity¹ 3.16 2.72 2.48

Incidence 22/25 19/25 19/25

Depression score

Mean of Day O to 14 0.02 0.03 0.02

Severity¹ 0.20 0.16 0.12

Incidence 5/25 4/25 3/25

Gauntness score¹

Mean of Day O to 14 0.19 0.14 0.14

Severity¹ 0.64 0.68 0.52

Incidence 14/25 14/25 11/25

Severity: Average of worst score observed for each pig over 14-d period.

Viral shedding

The effects of narasin levels (0, 30, 60 mg/kg) on within-day viral shedding of nursery pigs (Table 4) and percentage of nursery pigs shedding PEDV (Table 5) are compared. Fecal swabs were collected from all pigs on test daily from Day 0 to 14 of study. Each sample was labeled with pig identification, pen number, and sample day. All samples were frozen at the time of collection and stored until required for analysis. Only fecal swab samples collected from days 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, and 14 were sent for analysis. Fecal swab samples were sent to the Iowa State Veterinary Diagnostic

Laboratory (ISVDL) and were analyzed using real-time RT-PCR to determine viral shedding of PEDV. Table 4. Least-squares means for the effects of narasin inclusion level within day on viral shedding of nursery pigs challenged with PEDV

-values

Item Narasin Day Narasin x Day

Viral shedding 0.01 <0.0001 <0.0001

Narasin inclusion level, mg/kg

Item 0 30 60

No. of pens 5 5 5

Viral shedding,

cells/mL

Day O 0 0 0

Day 1 1 1 0

Day 2 802,918 1,005* 1 *

Day 3 46,321,178 152,889* 4,085*

Day 4 299,600,217 7,543,717 18,980*

Day 5 2,577,353,893 108,303,640 593,842*

Day 6 2,546,739,463 879,972,048 5,551,647*

Day 7 2,642,072,514 1,422,120,182 171,586,154

Day 8 83,710,799 268,967,479 58,813,444

Day 9 5,615,075 63,817,042 16,189,481

Day 14 3,665 2,256 9,262

Within day, means are significantly different than control treatment (P < 0.10).

Values were ln(count + 1) transformed prior to the statistical analysis.

²Values presented are only from pigs testing positive for shedding. Values for pigs testing negative (i.e., 0) are not included in the data set.

When compared to the control, pigs fed 30 mg/kg narasin had lower (P < 0.10) viral shedding on Day 2 and Day 3 of study, and consistently had numerically lower viral shedding through Day 7 of study. Pigs fed 60 mg/kg narasin had lower (P < 0.10) viral shedding on Day 2, 3, 4, 5, and 6 of study, and had numerically lower viral shedding on Day 7 and 8 of study (Table 4).

There was no effect (P > 0.10) of narasin level on the percentage of pigs shedding PEDV, but the duration of shedding generally decreased as narasin level increased. Histology

The effects of narasin inclusion level on the intestinal histology score and immunohistochemistry were analyzed. As narasin level increased from 0, 30, 60 mg/kg), histology scores decreased from 2 to 0 while the immunohistochemistry score decreased only at the 60mg/kg level (from 3 to 2) although differences were not significant (P > 0.05).

Claims

WHAT IS CLAIMED IS:

1. A method of treating porcine epidemic diarrhea virus (PEDV) infection in a nursery pig, comprising administering to said pig narasin with an orally- acceptable carrier.

2. The method of Claim 1, wherein the orally-acceptable carrier is selected from the group comprising an animal feed, a liquid composition other than an animal feed, and a solid composition other than an animal feed.

3. The method of Claim 1 or 2, wherein the concentration of narasin is selected from the group of about 30 mg/kg, about 40 mg/kg, about 50 mg/kg, and about 60 mg/kg of the composition.

4. A method of treating porcine epidemic diarrhea virus (PEDV) infection in a nursery pig, comprising administering to said pig narasin with an animal feed, wherein narasin is present at a concentration of about 60 mg/kg of the animal feed.

5. Narasin for use in the treatment of PEDV infection in a nursery pig.

6. Narasin for use in the treatment of PEDV infection in a nursery pig, wherein narasin is in a composition with an orally-acceptable carrier selected from the group comprising an animal feed, a liquid composition other than an animal feed, and a solid composition other than an animal feed.

7. The composition of Claim 5, wherein narasin is present at a concentration of about 30 mg/kg, about 40 mg/kg, about 50 mg/kg, and about 60 mg/kg of the orally-acceptable carrier. A composition for providing an antiviral effect to a nursery pig, the composition comprising a concentration of narasin and an orally-acceptable carrier.

The composition of Claim 8, wherein the orally-acceptable carrier is selected from the group comprising an animal feed, a liquid composition other than an animal feed, and a solid composition other than an animal feed.

The composition of Claim 8, wherein the concentration of narasin is selected from the group of about 30 mg/kg, about 40 mg/kg, about 50 mg/kg, and about 60 mg/kg of the composition.